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121,890 results • Page
11 of 2438
Sort: Rank
Rank
Views
Votes
Replies
1
vote
2
replies
482
views
Difficulties in calling peaks for CUT&RUN (IgG control with high RPKM value)
CUTRUN
calling
IgG
peak
11 weeks ago by
Basti
★ 2.1k
7
votes
3
replies
744
views
custom BED to UCSC genome browser
browser
ucsc
ucsc-genome-browser
genome
methylation
bed
12 weeks ago by
npont
▴ 20
1
vote
2
replies
482
views
unmatched number of reads after trimming treatment by afterqc
NGS
genome
assembly
12 weeks ago by
德水
• 0
0
votes
1
reply
466
views
Extract Specific RNA-seq reads from BAM using deeptools
RNA-seq
deeptools
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
Qilin
• 0
0
votes
11
replies
970
views
Error Correction with Tadpole and BBMerge
BBmerge
tadpole
error
correction
12 weeks ago by
Jon
• 0
2
votes
1
reply
390
views
Quantification for small RNAseq data
quantification
seq
data
smallRNA
updated 12 weeks ago by
rfran010
★ 1.6k • written 12 weeks ago by
ZuelTech
• 0
6
votes
4
replies
734
views
GrCh37 or GrCh38? That is the question.
GrCh37
sequence
human
genome
GrCh38
11 weeks ago by
Anjan
▴ 840
0
votes
2
replies
635
views
Scvi - Integration
integration
singlecell
scvi
11 weeks ago by
t.fosk
• 0
7
votes
3
replies
603
views
Bootstrapping in RNA-seq
bootstrapping
RNAseq
updated 12 weeks ago by
rfran010
★ 1.6k • written 12 weeks ago by
littlebioinformatician
• 0
1
vote
2
replies
569
views
Computing ka/ks ratio for individual genes.
ks
ka
evolution
selection
11 weeks ago by
Shakunthala Natarajan
• 0
1
vote
0
replies
1.4k
views
Job:
Several Permanent Positions as Bioinformatician/Computational Biologist/System Developer/Project Leader at Swedish national research infrastructures
Sweden
SciLifeLab
Genomics
Uppsala
Proteomics
11 weeks ago by
Matthias Zepper
5.1k
2
votes
2
replies
492
views
Obtaining a BED/GTF from Ensembl
rna-seq
ensembl
bcftools
rna
12 weeks ago by
joe_genome
▴ 70
0
votes
0
replies
582
views
News:
New Bioconductor and Physalia Collaboration!
Bioconductor
DataAnalysis
Genomics
12 weeks ago by
Physalia-courses
★ 2.6k
1
vote
1
reply
466
views
Read1 and read2 asymmetry in stranded, paired-end rnaseq data aligned by STAR
stranded
STAR
RNAseq
antisense
sense
updated 12 weeks ago by
rfran010
★ 1.6k • written 12 weeks ago by
yampolsk
▴ 10
0
votes
1
reply
552
views
Does the order of SplitNCigarReads and MarkDuplicates affect RNA-seq variant calling results?
variantcalling.
rnaseq
gatk
updated 12 weeks ago by
rfran010
★ 1.6k • written 12 weeks ago by
iamsmor
• 0
0
votes
0
replies
331
views
Should I standardize age and age2 as covariates in GWAS models?
GWAS
covariates
12 weeks ago by
yu
• 0
5
votes
6
replies
832
views
Venn Diagram
VennDiagram
updated 12 weeks ago by
lieven.sterck
15k • written 12 weeks ago by
Nasim Gandomdoust
• 0
0
votes
1
reply
400
views
PhageTerm error
phage
genome
phageterm
assamble
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
NIkita
• 0
0
votes
1
reply
388
views
WGCNA Workflow from GEO FASTQ Files – Expression Type, Sample Inclusion, and Preprocessing
fastq
wgcna
rna
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
tutorwhizzz
• 0
0
votes
0
replies
290
views
small RNA-Seq pipeline Standstill
NGS
miRNA
12 weeks ago by
anthony.santana.703.j
▴ 30
2
votes
3
replies
510
views
comparison interpretation
model-matrix
contrast
design-matrix
9 weeks ago by
jkim
▴ 220
0
votes
0
replies
275
views
piRNAs Analysis Pipelines
piRNAs
smallRNA
12 weeks ago by
GA
• 0
1
vote
1
reply
420
views
Beagle PATH (partially) recognised on Ubuntu 22.04
Ubuntu
Beagle
Beast
MCMC
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
Luca Arbore
▴ 10
0
votes
0
replies
294
views
CNV Computation with HoneyBadger
CNV
HoneyBADGER
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
mete.han.celebi
• 0
0
votes
0
replies
271
views
How to predict programatically TFBS and calculate PWM Score as JASPAR
PWMScan
TFBS
JASPAR
12 weeks ago by
t.kajiyama
• 0
0
votes
14
replies
1.2k
views
Host Removal Issues Human/Dog with samples containing Eukaryotic species
Mapping
Eukarotic
Host
updated 10 weeks ago by
Ram
45k • written 12 weeks ago by
Jon
• 0
1
vote
1
reply
556
views
Pharokka Error
error
annotating
viral
pharokka
genome
updated 12 weeks ago by
Mensur Dlakic
★ 30k • written 12 weeks ago by
NIkita
• 0
0
votes
0
replies
308
views
Combining Metatranscriptomics (Mtx) and Metagenomics (Mgx)
metagenomics
reference-based
Metatranscriptomics
alignment
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
rk009
• 0
1
vote
1
reply
381
views
how to make a circular plot of variants
circular
plot
updated 12 weeks ago by
Pierre Lindenbaum
166k • written 12 weeks ago by
analyst
▴ 70
2
votes
6
replies
673
views
GSEA analysis
RNA-seq
RNA
analysis
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
Ahmed
• 0
0
votes
1
reply
356
views
how to make go term plot and kegg pathway plot using InterProScan output
interproscan
10 weeks ago by
analyst
▴ 70
1
vote
3
replies
745
views
Why little difference in RNAseq alignment when flipping forward and reverse strand with paired end reads
mRNA
rna-seq
bowtie
alignment
updated 12 weeks ago by
swbarnes2
15k • written 12 weeks ago by
JourneyToAbyss
▴ 250
0
votes
1
reply
395
views
Questions about sample_accession_id and file_accession_id from EGA files
EGA
open
WGS
data
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
askif4
▴ 20
4
votes
4
replies
673
views
Example of ClinVar pathogenic variant where the reference allele is pathogenic?
snp
variant
pathogenic
clinvar
11 weeks ago by
a615ebfb
▴ 60
0
votes
1
reply
368
views
Functional Analysis Using EMU Output – Has Anyone Tried This?
emu
updated 12 weeks ago by
andres.firrincieli
3.9k • written 12 weeks ago by
henrique.mouradias
• 0
1
vote
3
replies
539
views
featureCounts -t option not working in v2.0.8?
subread
featureCounts
RNAseq
updated 12 weeks ago by
rfran010
★ 1.6k • written 12 weeks ago by
atan
• 0
0
votes
1
reply
443
views
mm10 blacklist regions detailed information
sequencing
DNA
blacklist
updated 12 weeks ago by
GenoMax
153k • written 12 weeks ago by
annaA
▴ 10
0
votes
2
replies
448
views
identify unmapped regions
human
illumina
libraries
12 weeks ago by
María José
▴ 10
0
votes
1
reply
500
views
martCheck - Error - You must provide a valid Mart object - for running HoneyBADGER for CNV computation
CNV
biomaRt
HoneyBADGER
12 weeks ago by
mete.han.celebi
• 0
0
votes
1
reply
425
views
How to Specify Power Parameter for Adjacency in modulePreservation() (WGCNA)
module
analysis
WGCNA
preservation
updated 12 weeks ago by
andres.firrincieli
3.9k • written 12 weeks ago by
Berkan
• 0
0
votes
1
reply
386
views
filters used in mutation discovery from RNAseq data
filter
RNAseq
mutation
updated 12 weeks ago by
GenoMax
153k • written 3 months ago by
htchd
▴ 20
4
votes
6
replies
787
views
Trouble Using GEO Files with Seurat
seurat
GEO
scRNA
updated 12 weeks ago by
antonioggsousa
3.4k • written 3 months ago by
Jamie
• 0
0
votes
0
replies
348
views
Knowledge Graph for AI
KnowledgeGraph
biotech
AI
SPOKE
Bioinformatician
3 months ago by
Cornelio
• 0
2
votes
2
replies
1.1k
views
How to convert from .spec to .bam?
bam
file-formatting
spec
updated 3 months ago by
Daniel Lai
▴ 10 • written 5.0 years ago by
gmora
▴ 30
2
votes
1
reply
432
views
Insert size is zero
rna-seq
fastp
insert
size
updated 3 months ago by
GenoMax
153k • written 3 months ago by
SpliceAndScript
• 0
0
votes
3
replies
579
views
Should matched samples (not paired) be included in the DESeq2 design model?
edgeR
limma
DESeq2
updated 12 weeks ago by
i.sudbery
22k • written 3 months ago by
marieke
• 0
0
votes
4
replies
607
views
Trajectory Analysis scRNA-seq with one cell type and two developmental stages
cellrank
palantir
pseudotime-trajectory-analysis
scrna-seq
trajectory-analysis
12 weeks ago by
npont
▴ 20
0
votes
1
reply
715
views
How to run trajectory analysis with only one cell type using palantir?
palantir
scanpy
updated 3 months ago by
npont
▴ 20 • written 14 months ago by
bioinfo
▴ 160
0
votes
1
reply
366
views
should I remove the transcripts from annotate peak region in ATAC-seq
ATAC-seq
updated 12 weeks ago by
rfran010
★ 1.6k • written 3 months ago by
QX
▴ 80
3
votes
2
replies
589
views
DESeq2 LRT test with multifactorial design
test
design
multifactorial
LRT
3 months ago by
lessismore
★ 1.4k
121,890 results • Page
11 of 2438
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Recent Replies
Comment: Yeast reference-based genome assembly
by
Michael
56k
So, you aren't sure about the exact species? Then you might want to be careful with reference-based assembly in general. I recommend the fo…
Comment: Structural Variant identification on pangenome graphs
by
Panos
★ 1.8k
That's a very comprehensive list! Thanks for sharing! `minigraph` better suits my needs because all I need is SVs for my genomes. As far a…
Comment: Yeast reference-based genome assembly
by
amy967107
• 0
I have ~2.01 Gb of ONT data and the target genome is ~20–23 Mb (90–100× coverage). My ONT read N50 is ~3.8 kb, so contiguity may be limited…
Comment: Yeast reference-based genome assembly
by
amy967107
• 0
This is a yeast strain (probably Rhodotorula spp.) and I'm trying to assemble the entire genome from nanopore reads using a reference-based…
Answer: Yeast reference-based genome assembly
by
Michael
56k
The new [hifiassm ONT][1] may be all you need for getting a good assembly. I would not recommend LRSDAY, except for its annotation part (wh…
Comment: magpurify errors
by
Mensur Dlakic
★ 30k
By the way, these errors are not unique. If you look through the `magpurify` GitHub issues, both types have been reported already. - https…
Comment: magpurify errors
by
Mensur Dlakic
★ 30k
There is absolutely no chance that a contig labeled `k127_4584534` doesn't exist in your fasta files. These names are not made up out of th…
Comment: magpurify errors
by
shevch2009
▴ 20
Strange but there are no such headers or contig names in my fasta files
Comment: replace gene names in gff file
by
Juke34
9.3k
Yes the --prefix Option exists. There is no count per chromosome. You can do it by splitting your input and analyse one sequence at a time…
Comment: Variant analysis for mouse WES
by
GenoMax
153k
You could open a new issue and ask the developers of `maftools` if this was something they can add.
Comment: How to Identify Conserved 21-mers Across TE Insertions in Drosophila?
by
GenoMax
153k
Do you have the locations/sequence of the regions you are interested in?
Comment: magpurify errors
by
shevch2009
▴ 20
Thank you
Comment: magpurify errors
by
Mensur Dlakic
★ 30k
To me that sounds like an error in sequence header formatting. Maybe some contig headers are repeated? Or their sequences are short or miss…
Comment: magpurify errors
by
shevch2009
▴ 20
Thanks What about phylo-markers module error, I tried to look for it :) But haven't found anything. And why it's not working for some but …
Answer: magpurify errors
by
Mensur Dlakic
★ 30k
A general answer is to always Google the error message. Hopefully you do that in the future. This is the outcome of Googling `AttributeErro…
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